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Senior Quality Assurance EngineerDormont Manufacturing Co • Redmond, Washington, United States
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Senior Quality Assurance Engineer

Dormont Manufacturing Co
  • US
    Redmond, Washington, United States
  • US
    Redmond, Washington, United States
Jetzt Bewerben

Über

Work Flexibility: Hybrid
Join Stryker as a
Senior Quality Assurance Engineer
in
Redmond, WA
Supporting In this role, you will help ensure that life‑saving medical devices meet the highest standards of quality and safety, while driving initiatives that enhance product performance and compliance, directly impacting patient outcomes worldwide. If you’re passionate about quality and continuous improvement, this is your opportunity to make a difference.
Work Flexibility: Candidates must reside within a commutable distance to Redmond, WA and be able to work onsite
4 days
per week.
What you will do
Ensure
quality performance of products and manufacturing processes across operations and key business functions.
Lead
internal and supplier nonconformance investigations, including problem definition, containment, root cause analysis, and timely closure against agreed due dates.
Manage
and prioritize multiple quality initiatives simultaneously, balancing competing priorities across cross‑functional partners.
Own
corrective and preventive actions (CAPA), including documentation, effectiveness checks, and on‑time completion through closure.
Review
and
approve
change control activities to support compliant implementation and sustained process performance.
Analyze
key performance indicator trends (e.g., defects, scrap, yield) and drive improvement actions to reduce waste and variation.
Support
process and equipment validation/qualification activities, including protocol review, execution support, and report approval.
Prepare
audit evidence and support internal/external audits, including response development and follow‑up actions within committed timelines.
Apply
risk management and human factors considerations to manufacturing operations, including risk assessments and mitigation planning.
What you will need Required
Bachelor’s degree in Science, Engineering, or a related discipline.
Minimum 2 years of experience in quality, manufacturing, or engineering; experience in regulated industries is a plus but not required.
Preferred
Knowledge of medical device manufacturing and quality system standards (e.g., ISO 13485, Good Manufacturing Practice).
Lean Six Sigma training or certification.
Experience with nonconformance management, CAPA, change control, and audit support.
Experience applying risk management tools and statistical methods (e.g., sampling plans, process capability, measurement system analysis, Gauge R&R).
Familiarity with regulatory bodies (e.g., FDA, notified bodies, Ministry of Health) and compliance expectations.
US15: $89,400 - $148,900 USD Annual
Travel Percentage: 10%
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability. Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.
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  • Redmond, Washington, United States

Sprachkenntnisse

  • English
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